A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605239



Internal ID16392648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164709839..164808840hg38UCSC Ensembl
Innerchr6:165130872..165222329hg19UCSC Ensembl
Innerchr6:165050862..165142319hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3899002
hg1991458
hg1891458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11034n54
Supporting Variantsnssv1075797, nssv1075796
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605239
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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